10379-52-9

Usage

Uses

Used in Pharmaceutical Applications:
(17α)-22,29,30-Trinor-A'-neogammaceran-21-one is used as a pharmaceutical agent for its potential antioxidant and anti-inflammatory properties. These properties make it a candidate for the development of treatments targeting various diseases and conditions where oxidative stress and inflammation play a role.
Used in Cosmetic Applications:
In the cosmetic industry, (17α)-22,29,30-Trinor-A'-neogammaceran-21-one is used as an active ingredient for its antioxidant and anti-inflammatory properties. It can be incorporated into skincare products to provide potential benefits such as reducing inflammation, promoting skin health, and protecting the skin from oxidative damage.
Used in Scientific Research:
(17α)-22,29,30-Trinor-A'-neogammaceran-21-one is used as a subject of scientific research for its unique chemical structure and potential biological activities. Researchers are interested in studying its properties and applications to further understand its potential uses in medicine and other fields.
Used in Product Development:
In the field of product development, (17α)-22,29,30-Trinor-A'-neogammaceran-21-one is used as a compound of interest for the creation of new products with potential health benefits. Its unique properties and potential applications make it a valuable component in the development of innovative products in various industries.

Upstream product

• 10379-54-1 hopane-21β,22-diol 
• 1981-81-3 hydroxyhopanone 
• 67-56-1 methanol 
• 1172-78-7 22,29,30-trinor(17αH)-hopan-21-one 
• 1615-92-5 hop-22⁽²⁹⁾-ene 
• 1615-92-5 hop-21-ene 
• 1172-78-7 trisnorhopanone 

Downstream Products

• 1172-78-7 17αH-trisnorhopanone 
• 33281-79-7 30-Nor-17α-hopan-22-one 
• 33281-19-5 isoadiantone 
• 81600-07-9 30-Nor-17α-moretane 
• 51271-94-4 17β(H)-22,29,30-trisnorhopane 
• 63543-60-2 22,29,30-trinor-28(18-> 17S)abeo-hop-13(18)-ene 
• 1172-78-7 22,29,30-trinor(17αH)-hopan-21-one 
• 90663-11-9 (1R,2R,4aR,4bR,6aS,10aS,10bR,12aR)-1,4a,4b,7,7,10a-Hexamethyl-1-vinyl-octadecahydro-chrysene-2-carbaldehyde 
• 82358-71-2 3-((1R,4aR,4bR,6aS,10aS,10bR,12aR)-1,4a,4b,7,7,10a-Hexamethyl-octadecahydro-chrysen-1-yl)-propionic acid methyl ester 

Relevant academic research and scientific papers

Seasonal fluctuation of triterpenoid constituents from dried leaflets of dryopteris crassirhizoma

Eight triterpenoids of the hopane and migrated hopane series, and a sterol mixture were isolated from the dried leaflets of Dryopteris crassirhizoma. Seasonal fluctuations in the levels of these compounds from June to October were correlated with biogenesis.

From Bio- to Geohopanoids: an Efficient Abiotic Passage Promoted by Oxygen in the Presence of Cuprous Chloride

In the presence of cuprous chloride, the representative biohopanoid 1a was smoothly converted by oxidation in pyridine into aldehydes, ketones and carboxylic acids with the same skeletons as those of molecular fossils ubiquitously found in the organic mat

UNEXPECTED REGIOSPECIFICITY IN PHOTOCHEMICAL α-CLEAVAGE OF HYDRINDANONES.

Triterpene derived trans-hydrindanones 1 of the hopane and lupane series undergo highly regiospecific photochemical α-cleavage; they are cleaved in high yields on the least substituted side of the ketone.The more stable cis-hydrindanones 1 exclusively cleave on the more substituted side as expected.

Synthesis of Biological Markers in Fossil Fuels. 1. 17α and 17β Isomers of 30-Norhopane and 30-Normoretane

21-Hydroxyhopan-3-one was converted to a mixture of 22,29,30-trinor-17α-hopan-21-one and 30-norhopan-22-one by the following reaction sequence: (1) dehydration with phosphorus oxytrichloride, (2) Wolff-Kishner reduction, and (3) ozonolysis.These two keton